The cell cycle, autophagy, and cell wall integrity pathway jointly governed by MoSwe1 in Magnaporthe oryzae

The cell cycle is pivotal to cellular differentiation in plant pathogenic fungi. Cell wall integrity (CWI) signaling plays an essential role in coping with cell wall stress. Autophagy is a degradation process in which cells decompose their components to recover macromolecules and provide energy under stress conditions. However, the specific association between cell cycle, autophagy and CWI pathway remains unclear in model pathogenic fungi Magnaporthe oryzae. Here, we have identified MoSwe1 as the conserved component of the cell cycle in the rice blast fungus. We have found that MoSwe1 targets MoMps1, a conserved critical MAP kinase of the CWI pathway, through protein phosphorylation that positively regulates CWI signaling. The CWI pathway is abnormal in the ΔMoswe1 mutant with cell cycle arrest. In addition, we provided evidence that MoSwe1 positively regulates autophagy by interacting with MoAtg17 and MoAtg18, the core autophagy proteins. Moreover, the S phase initiation was earlier, the morphology of conidia and appressoria was abnormal, and septum formation and glycogen degradation were impaired in the ΔMoswe1 mutant. Our research defines that MoSWE1 regulation of G1/S transition, CWI pathway, and autophagy supports its specific requirement for appressorium development and virulence in plant pathogenic fungi. Video Abstract Supplementary Information The online version contains supplementary material available at 10.1186/s12964-023-01389-6.


Introduction
Magnaporthe oryzae differentiates specialized infection structures-appressoria to breach the plant cuticle, which is the causal agent of rice blast disease in cereal plants [46,56,64,75].During the appressoria maturation, the nuclei of conidia are degraded via the autophagy pathway; then, the overall conidia contents are transported to appressoria [68].In the process of continuous accumulation of turgor pressure to the maximum 8 MPa [24], the appressoria dynamically remodel their actin cytoskeleton, thereby forming a circular F-actin network at the base of the appressorium.Septin GTPases support F-actin and form a penetrating peg at the base of the appressorium to penetrate plant leaves [11].When the three-cell conidia germinate, the apical cells undergo only one round of mitosis.One nucleus divides to form two nuclei, one entering the appressorium and the other returning to the apical cell.The basal cell and the middle cell do not undergo mitosis and septum formation.When the appressorium matures, each nucleus is degraded by autophagy, resulting in cell death of the conidia and recycling of the conidia bulks into the appressoria [28,52].
The eukaryotic cell cycle is a highly coordinated and conserved process.The cell cycle and cell division cooperate to regulate fungal morphogenesis, including the stage of conidial germination and the location of appressorial penetration of plants [15,61].In Colletotrichum orbiculare, appressorium formation is required for suitable cell cycle progression, which CoBub2 and CoBfa1 regulate.Disruption mutants initiate earlier G1/S progression during conidial germination [16].In M. oryzae, the ability of appressoria to infect plants is closely related to cell cyclemediated regulation [53,62].Appressoria development and the emergence of penetration pegs depend on the synthesis phase (S phase) of the cell cycle [52,61].Recent studies have shown that rice blast infection is controlled by two independent S-phase checkpoints operating in two successive cell cycles.The first checkpoint occurs during the initial stages of appressoria formation and is related to the DNA damage response (DDR) pathway, with MoCds1 kinase involvement.The second checkpoint is controlled in a completely different way by the turgor pressure of the appressorium, which controls NADPH oxidase activation and the remodeling of septindependent F-actin at the base of appressoria.This process regulates the emergence of the penetration peg and leads to plant infection [53].
In S. cerevisiae, Swe1 (S. cerevisiaewee1 homolog) inhibits the activity of Cdk1/Cdc28-Clb2 through phosphorylation of Y19 (the 19th amino acid site of tyrosine) of Cdk1 [7].This modification process can be reversed by dephosphorylation of Mih1 [59].Swe1 controls the timing of entry into mitosis in S. cerevisiae [27].Swe1 appears for the first time in the nucleus of the late G1 phase.Swe1 is localized to the daughter bud side of the mother bud neck in a form-dependent Hsl1 kinase and Hsl7 protein when the bud appears [39].Before late G2 is degraded, Swe1 in the bud neck is hyperphosphorylated by Cdc5, Cla4, and Cdk1-Clb2 proteins [1,21,23,48,60].The hyperphosphorylated form of Swe1 is susceptible to ubiquitination and can be degraded by the 26 S proteasome [48].In S. cerevisiae, the primary function of the three kinase proteins (Hsl1, Kcc4, Gin4) is to transfer Swe1 to the bud neck, facilitating Swe1 degradation and the subsequent cell cycle.Moreover, the functions of the three kinase proteins are different [41,50].Gin4 and Kcc4 cooperate with the PAK kinase Cla4 to participate in the reorganization of septin, and Hsl1 is directly involved in the degradation progression of Swe1 [3,9].In M. oryzae, Gin4 (MGG_02810) is a homologous protein of Nim-related kinase and arginine N-methyltransferase Hsl7 (MGG_03894) localized in appressoria pores before the infection of plants [52].However, how the mitosis progression is regulated remains unclear.
In this study, we demonstrated the functions of MoSwe1 in conidium, appressorial morphogenesis, appressorial differentiation, septum formation, and plant invasion in M. oryzae.Our results found that MoSwe1 positively regulates the CWI pathway by affecting MoMps1 phosphorylation levels.In addition, MoSwe1 interacts with autophagy proteins MoAtg17 and MoAtg18 to regulate autophagy.We report here a novel link, namely MoSwe1 linkage of cell cycle control, CWI signaling, and autophagy, that underlies the growth and pathogenicity of rice blast fungus.

Identification of Swe1 in M. oryzae
To explore the functions of Swe1 in plant pathogenic fungi, we acquired the sequences of MoSwe1 in M. oryzae.Taking the S. cerevisiae Swe1 protein as a query, MGG_01816 was identified as the homolog of the Wee protein kinase Swe1 through a search of the M. oryzae genome database EnsembIFungi (http:// fungi.ensem bl.org/ Magna porthe_ oryzae/ Info/ Index?db= core).MGG_01816 shows 30.62% identity with ScSwe1.Thus, MGG_01816 was named MoSwe1.We cloned the full-length Swe1 cDNA sequence, which encodes an 1110 amino acid protein in M. oryzae.Sequence alignment supported that the Swe1 protein is well conserved among eukaryotes (Fig. S1A).The results showed that the MoSwe1 protein shares 44.01%amino acid identity with the homologous protein in C. orbiculare, 42.41% identity with the homologous protein in Fusarium graminearum, 38.03% identify with that in Aspergillus fumigatus, 43.03% identify with that in Fusarium oxysporum, 32.08% identify with that in Mus musculus, and 32.27% with that in Homo sapiens.We predicted the protein structure of Swe1 by AlphaFold2.We found that Swe1 had conserved regions in M. oryzae (Fig. S1B), consistent with the amino acid sequence alignment results shown in Fig. S1A.

Swe1 functions in G1/S progression by regulating Cdc28 phosphorylation
To characterize the functions of MoSwe1, we replaced the Swe1 protein coding sequence with a glufosinateammonium resistance gene (BAR) to produce ΔMoswe1 deletion mutant (Fig. S2).The Swe1/Wee1 kinase phosphorylates and inhibits Cdk1(Cdc28)-Clb2, a primary mitotic switch in yeast [59].To determine whether MoSwe1 regulates the Cdc28 phosphorylation and cell cycle progression, we demonstrated the interaction between MoSwe1 and MoCdc28 through yeast two-hybrid system and bimolecular fluorescence complementation (BiFC) experiments (Fig. 1A and B).We used P-cdc2 (Tyr15) antibody to study MoCdc28 (Cdc2 Western blot was carried out to detect Cdc28 Y15 (for phosphorylation signal) and Cdc28 in protein extracts using the anti-phospho-Cdc28 (Tyr15) and anti-Cdc28 antibodies, respectively homolog) phosphorylation in the wild type 70 -15 and the ΔMoswe1 mutant and found that MoCdc28 phosphorylation levels were lost entirely in the ΔMoswe1 mutant (Fig. 1C).Data from the quantitative phosphoproteomic data also showed a complete loss of MoCdc28 (Tyr15) phosphorylation in the ΔMoswe1 mutant (Fig. 8F).These results indicated that MoSwe1 affects the phosphorylation of MoCdc28.
It is well known that the S phase of mitosis carries out DNA replication and synthesis, controlling initial appressorial development and the emergence of penetration pegs in many pathogenic fungi [53,62].When a particular concentration of DNA replication inhibitor Hydroxyurea (HU) is added to the germinating conidia, initial appressoria cannot be formed.In addition, when HU was used to treat mature appressoria, the formation of penetration pegs and plant infection were blocked in M. oryzae [53,62].To further explore the specific mitotic processes (G1 phase, S phase, G2 phase, M phase) affected by MoSwe1, we collected conidia of the 70-15, ΔMoswe1 and ΔMoswe1-C strains to induce appressoria on hydrophobic coverslips.HU was added to the ΔMoswe1 mutant at 2 h post-incubation (hpi), and almost no appressoria had formed at 24 hpi (Fig. S3A and B).The phenotype of the ΔMoswe1 mutant was consistent with that of the 70-15.The data showed that the ΔMoswe1 mutant is not sensitive to HU and that MoSwe1 does not directly participate in determining the S phase of the cell cycle.
To study whether the nuclear division was affected in the ΔMoswe1 mutant during conidial germination, red fluorescent nuclear localization proteins (NLS-mCherry) were used to observe dynamic changes in the nucleus in the 70-15 and the ΔMoswe1 mutant.We first observed differences in nuclei during conidial germination.Surprisingly, in the ΔMoswe1 mutant, two nuclei appeared in the basal cells and the middle cells of conidia during conidia germination (Fig. 2A).In contrast, in the wild type 70-15, nuclear division occurs only in apical cells.Nuclear division in the ΔMoswe1 mutant occurs in the apical cells and the middle and basal cells, resulting in binucleate cells.To more accurately and intuitively understand the difference between cell nuclear division in the ΔMoswe1 mutant and wild type 70-15, we counted the nuclei in a conidium, in one cell, and in an appressorium at different periods of conidial germination (Fig. 2B).The statistical data showed that the proportion of cells with two nuclei in a conidium during conidium germination was more than 20%.Still, there was only one nucleus in one cell in a conidium in the wild type 70-15 and ΔMoswe1-C complemented strain (ΔMoswe1-C) (Fig. 2B).In addition, during conidial germination and appressorium formation, the number of nuclei in the conidium and appressorium were counted.At 0 hpi, 4 hpi, and 8 hpi, respectively, the proportion of conidia containing more than three nuclei was more than 70% in the ΔMoswe1 mutant compared with the 70-15 and ΔMoswe1-C strains, whose conidia did not have more than three nuclei (Fig. 2C).The proportion of appressoria with two nuclei in the ΔMoswe1 mutant was more than 20% at 8 hpi and 24 hpi, while there were no binucleate appressoria in the wild type 70-15 and ΔMoswe1-C (Fig. 2D).We also measured the level of nucleus degradation at protein levels.mCherry antibody was used to detect the degradation level of nuclear protein H2B.We found that H2B-mCherry was always present in the ΔMoswe1 mutant (Fig. 2E).This indicated that the cell nuclei in the ΔMoswe1 mutant did not degrade.
Next, we further examined the timing of cells entering the S phase during conidial germination to determine whether earlier nuclear division in the ΔMoswe1 mutant was due to earlier progression in the cell cycle G1/S transition.We introduced chromosome tagging into the wild type 70-15 and the ΔMoswe1 mutant.Yasuyuki Kubo's group developed a method to detect the specific phase of mitosis by constructing a plasmid consisting of an array of 256 Lac operator repeats inserted into the locus of an individual chromosome in the genome and GFP-LacI-NLS fusion sequences.After the plasmid is transformed into the target strain, only one GFP point indicates that the cell is in the prereplication stage (G1).If two GFP spots are present, the cell is in the S/G2 phase, and these two spots are located on the sister chromatids [17].Using this method, we observed the cell cycle progression of the basal cells, middle cells, and apical cells of the conidia and the cells of the appressoria in M. oryzae.At 0 hpi, two GFP spots were present in the middle and basal cells of the ΔMoswe1 mutant, whereas only one GFP spot was present in all wild type 70-15 cells.The results indicated that the middle and basal cells of the ΔMoswe1 mutant had entered the S phase (Fig. 3A).At 3 hpi, only the apical cells had two GFP spots in wild type 70-15 (Fig. 3A), indicating that only the apical cells entered S phase.
In contrast, the basal and middle cells did not enter the S phase.However, in the ΔMoswe1 mutant, the apical cells and the middle and basal cells contained two GFP spots (Fig. 3B and D).At 24 hpi, the appressoria matured, and 30% of the appressoria of the ΔMoswe1 mutant had four GFP spots, indicating that the nucleus in the ΔMoswe1 mutant entered a second round of the S phase (Fig. S3C and D).Overall, the findings indicated that the G1 arrest was released immediately after the cells entered the G1 phase in the ΔMoswe1 mutant.In other words, knocking out MoSWE1 affects the G1/S phases of the cell cycle by regulating MoCdc28 phosphorylation of M. oryzae.

MoSWE1 affected vegetative growth, conidiogenesis, conidial and appressorial morphology, and appressorium formation of M. oryzae
To determine whether MoSwe1 is associated with vegetative growth in rice blast fungus, we observed the colony morphology of the ΔMoswe1 mutant on complete medium (CM), minimal medium (MM), oatmeal agar medium (OMA), and V8 vegetable juice (V8) medium (Fig. 4A).Compared with the wild type 70-15, the colony size of ΔMoswe1 was significantly reduced on CM, MM, OMA, and V8 medium after 9 days of growth.The ΔMoswe1-C recovered the defects of the ΔMoswe1 mutant (Fig. 4B).To further understand whether MoSwe1 is also involved in appressorium development, the ratios of appressorium formation in 70-15, ΔMoswe1 and the ΔMoswe1-C were determined at 4, 6, 8 and 24 hpi (Fig. 4C).At 4 hpi, barely 2.31% of the conidia in the ΔMoswe1 mutant could form appressoria, compared with 34.67% in the wild type 70-15.At 24 hpi, the ratio of appressorium formation in ΔMoswe1 increased to 47.79%.However, there were still significant differences compared with the proportions of appressorium formation in the 70-15 and ΔMoswe1-C, which exceeded 90% (Fig. 4D).The data showed that MoSWE1 is indispensable for fungal vegetative growth and appressorium formation in M. oryzae.
Since conidia are the spearhead of the spread of M. oryzae, we also evaluated the role of MoSwe1 in conidiation and conidial morphology.Conidia from 70-15, ΔMoswe1, and the ΔMoswe1-C were collected at 8 days-post-incubation (dpi) after culture on CM plates.We found that the wild type 70-15 conidiation was approximately 500 times that of the ΔMoswe1 mutant.This result indicated that the conidiation of the ΔMoswe1 mutant decreased sharply (Fig. 4E).Interestingly, via CFW staining, we found that septum formation was significantly impaired in the ΔMoswe1 mutant.Compared to more than 80% of conidia with two septa in wild type 70-15, conidia in the ΔMoswe1 mutant contained up to 3, 4, and 5 septa.This damage was fully recovered in the ΔMoswe1-C (Fig. 4F).As is shown in Fig. 4G, the percentage of conidia containing 4 cells, 5 cells, and 6 cells in the ΔMoswe1 mutant made up almost 50% of the total conidia.In addition, the appressorial morphology in the ΔMoswe1 mutant was changed.The appressoria of the ΔMoswe1 mutant were smaller than those of 70-15, and the ΔMoswe1-C.The wild type 70-15 appressoria were ~ 10 μm, while the diameter of the ΔMoswe1 mutant appressoria was only ~ 6 μm (Fig. 4H and I).Overall, the results clarified that MoSWE1 plays essential roles in conidial septum formation and conidial and appressorial morphology in M. oryzae.

MoSwe1 is involved in pathogenicity in M. oryzae
To study the role of MoSWE1 in M. oryzae, we tested the virulence of the wild type 70-15 strain, ΔMoswe1 mutant and the ΔMoswe1-C on detached susceptible rice seedling leaves and (Oryza sativa cv.CO-39) and barley leaves (Hordeum vulgare cv.ZJ-8).The ΔMoswe1 mutant showed fewer lesions than the wild type 70-15 and the ΔMoswe1-C (Fig. 5A and B).Furthermore, we found that the disease spots on barley leaves inoculated with the ΔMoswe1 mutant did not extend (Fig. 5C), indicating that MoSwe1 affected the invasive growth of rice blast fungus.We found that the ΔMoswe1 mutant almost did not infect rice leaves (Fig. 5D), and the disease spots caused by the ΔMoswe1 mutant on rice leaves were virtually ignored (Fig. 5E).In addition, microscopic observations confirmed that almost all types of invasive hyphae (IH) in ΔMoswe1 were type 1 (type 1, no IH; type 2, 1-2 IH; type 3, at least 3 short IH; type 4, abundant IH) at 48 hpi, indicating that the ΔMoswe1 appressoria barely penetrated plants, whereas more than 90% of the IH in 70-15 and the ΔMoswe1-C were types 3 and 4 (Fig. 5F and G).Moreover, it was found that the appressorial collapse rate of the ΔMoswe1 mutant was dramatically higher than those of the 70-15 and ΔMoswe1-C (Fig. 5H and I).The appressorial collapse rate of the ΔMoswe1 mutant was 78.15% compared with collapse rate of 51.14% in the wild-type 70-15 when the concentration of glycerol up to 1.5 M. Based on these experimental results, we concluded that MoSwe1 take on crucial roles during M. oryzae infection.

MoSwe1 interacts with MoAtg17 and MoAtg18 and regulates autophagy
To further elucidate the regulatory mechanism of MoSwe1, we conducted yeast two-hybrid (Y2H) assays to identify potential interactions.Concurrently, Y2H assays with a series of truncated MoSwe1 constructs revealed that the protein kinase C-terminal domain is essential for MoSwe1-MoAtg17 and MoSwe1-MoAtg18 interactions (Fig. 6B and E).Since the C-terminal domain of MoSwe1 is necessary for the interaction, we generated a MoSwe1-N2-GFP complemented construct (a truncated MoSwe1 containing a C-terminal domain [726-1110 aa] fused with GFP).We transformed it into ΔMoswe1 to investigate the function of the protein kinase C-terminus.The strain ΔMoswe1-N2-GFP displayed reduced mycelial growth on CM, although the growth defect was not as severe as that of ΔMoswe1 (Fig. S4A).In addition, the pathogenicity of the ΔMoswe1-N2-GFP strain did not fully recover and was only slightly more potent than that of ΔMoswe1 (Fig. S4B).Next, we carried out a pull-down experiment, and the results further verified the interaction between MoSwe1 and MoAtg17, and MoAtg18 (Fig. 6A and D).To find out MoSwe1 with MoAtg17 as well as the relationship between MoAtg18, we used a BiFC experiment to verify the interaction of MoSwe1 with MoAtg17 (Fig. 6C) and MoAtg18 (Fig. 6F).Taken together, these results convincingly demonstrated that MoSwe1 physically interacts with MoAtg17 and MoAtg18 in M. oryzae.
Studies have shown that the infection-associated nuclear degradation in M. oryzae, which is required to cause rice blast disease, occurs by non-selective autophagy [22].To examine whether MoSwe1 is necessary for the autophagy process, we evaluated autophagic activity by a survey of GFP-MoAtg8 processing.When cultured in CM medium (0 h), GFP-MoAtg8 fluorescence spots in the wild type 70-15 were mainly located in the cytoplasm near the vacuole.In contrast, GFP-MoAtg8 fluorescence spots in the ΔMoswe1 mutant were primarily located in the vacuole.After 4 h induction with nitrogen starvation medium (SD-N) medium, a small fraction of GFP-MoAtg8 fluorescence spots were found in the cytoplasm.They did not degrade into vacuoles in the wild type 70-15.In the ΔMoswe1 mutant, GFP-MoAtg8 fluorescence spots were located in the vacuole, and almost no dots were in the cytoplasm (Fig. 7A).
We collected conidia of wild type 70-15 and the ΔMoswe1 mutant to observe the autophagy processes associated with infection during appressorium development.GFP-MoAtg8 was mainly located in the cytoplasm from 0 to 4 h, and almost no fluorescence spots were observed in the cytoplasm at 8 h in the wild type 70-15.In the ΔMoswe1 mutant, there were very few fluorescent spots in the cytoplasm from 0 to 12 h (Fig. 7B).We then examined the autophagic flux in wild type 70-15 and the ΔMoswe1 mutant.In the wild type 70-15, the degradation of GFP-MoAtg8 was inhibited under the condition of nutrition, but the content of free GFP in the ΔMoswe1 mutant was higher than that in the wild type 70-15.The results indicated a significant increase in autophagy flow in the ΔMoswe1 mutant.After 4 h of starvation induction with SD-N medium, the bands of GFP-MoAtg8 in the ΔMoswe1 mutant almost disappeared (Fig. 7C), indicating that the autophagy process was accelerated and the autophagy was maintained at a high level in the ΔMoswe1 mutant.We also investigated the turnover of MoAtg8/ MoAtg8-PE, and we found that the lipidation level of MoAtg8 in the ΔMoswe1 mutant was significantly higher than that of the wild type 70-15 (Fig. 7D).This suggests that MoSwe1 negatively regulates autophagy.

MoSwe1 interacts with MoMps1 and affects the phosphorylation of MoMps1
We have demonstrated that MoSwe1 affects MoCdc28 phosphorylation as a kinase in M. oryzae.To explore whether MoSwe1 affects phosphorylation levels in other pathways, we carried out quantitative phosphoproteomic analyses.Phosphoproteins were purified from ΔMoswe1 and 70-15 by liquid chromatography with tandem mass spectrometry (LC-MS/MS).The data revealed MoSwe1dependent phosphorylation of proteins associated with the cell cycle, autophagy, and MAPK cascade (Fig. 8A).
As shown in the radar map of differentially modified sites (Fig. 8B), proteins with significantly different relative expression levels at differentially modified sites were divided into 4 categories.Among the 7 related proteins in the CWI pathway, PKC1 and MGG_03048 were significantly up-regulated, while RHO3, MGG_03481, MCK1, MPS1, and MKK2 were significantly down-regulated.All proteins related to the cell circulation pathway were significantly up-regulated except CDC28.In autophagy pathway, ATG28, VPS4, VPS74, MGG_06476, SEC24 were significantly up-regulated, ATG1, ATG13, ATG18,  VPS9, TOR and VPS54 were significantly down-regulated.Through protein interaction network analysis, it was found that autophagy pathway-related proteins and MAPK pathway-related proteins had an interaction relationship.Still, the two pathway-related proteins had no interaction relationship with cell cycle pathway-related proteins (Fig. 8C).
Based on the phosphoproteomic data, we speculated that MoSwe1 affected the MAPK pathway.Sensitivity tests showed that the ΔMoswe1 mutant grew faster in the medium containing 0.005% sodium dodecyl sulfate (SDS) and 400 ug/ml Congo red (CR), and the ΔMoswe1 mutant showed higher resistance to SDS and CR (Fig. 9A and B).We then used P-p44/42 antibody and found that MoMps1 phosphorylation levels were significantly reduced in the ΔMoswe1 mutant.According to the phosphoproteomic data, the phosphorylation levels of MoMps1 thr186 and tyr188 sites were downregulated considerably (Fig. 9D).MoMps1 in M. oryzae was homologous to Homo sapiens Erk2.The thr186 and tyr188 protein sites of MoMps1 (Fig. 9E) were consistent with the thr185 and tyr187 protein sites of Erk2 (Fig. 9F), respectively.The anti-phospho-p44/42 MAPK antibody (P-p44/42) detects p44 and p42 MAP kinases (Erk1 and Erk2) at endogenous levels after thr202 and tyr204 (Thr185 and Tyr187 of Erk2) double phosphorylation and after thr202 monophosphorylation [12,58].The interaction between MoSwe1 and MoMps1 was proved by the BiFC experiment (Fig. 9G) and yeast two-hybrid (Fig. 9H).In conclusion, we suggest that MoSwe1 interacts with MoMps1 to influence the infection and pathogenicity of M. oryzae by inhibiting the phosphorylation of MoMps1 185T and 187Y sites.

MoSwe1 affects septin ring assembly at the appressorium pore in M. oryzae
The cell cycle regulates septin ring formation, and the septin ring affects appressorial penetration [61].In M. oryzae, septin ring assembly affords a scaffold for the annular F-actin network at the appressorium pore [11].Therefore, studying the septin ring assembly can clarify the relationship between cell cycle progression and appressorial penetration.We speculated that MoSwe1 affects septin dynamics at the appressorium pore, which results in the penetration defect of the ΔMoswe1 mutant in the rice blast fungus.We expressed MoSep5-GFP in the wild type 70-15 and the ΔMoswe1 mutant to investigate this hypothesis.The wild type 70-15 formed a bright ring at the appressorium pore.In contrast, the ΔMoswe1 mutant formed an aberrant ring instead of the typical Fig. 8 Phosphorylation difference between 70-15 and ΔMoswe1 mutant was analyzed by phosphoproteome.A After GO classification, KEGG pathway, protein domain, Reactome, and WikiPathways enrichment, cluster analysis was conducted to find differences and similarities in the function of differentially expressed modified proteins between the comparison groups.There were three replicates of 70-15 and the ΔMoswe1 mutant.SW represents ΔMoswe1 mutant, and WT represents wild type 70-15.B We used radar maps to show the proteins that significantly expressed the autophagy, CWI, and cell cycle pathways among the differentially expressed proteins.From the outside to the inside, the first circle represents multiple differential proteins; the second circle orange arrow represents the sequence of differential proteins from small to large according to the P value; the third circle represents the ratio of differential expression change in the comparison group of Log2 conversion; pink represents up-regulation, blue represents down-regulation; the more significant the dot, the larger the multiple of difference.The fourth circle represents the average quantitative value of the two groups.C The differentially expressed proteins in the CWI pathway, autophagy pathway, and cell cycle were screened out from the significantly differentially expressed proteins.After comparing with the STRING protein interaction network database, the differentially modified protein interaction was extracted according to the confidence score > 0.7 (high confidence).Circles represent differentially modified proteins, blue are down-regulated modified proteins, red are up-regulated modified proteins, yellow is modified proteins that contain both up and down-modified sites, and the size of the circles indicate the number of proteins with which they interact central septin ring in the appressorium pore (Fig. S4C  and D).The results showed that the septin ring assembly in the appressorium pore was disrupted in the ΔMoswe1 mutant.

Glycogen and lipid utilization and degradation are attenuated in the ΔMoswe1 mutant
In M. oryzae, efficient utilization and transfer of glycogen and lipids contained in conidia are necessary for the appressoria to penetrate plant leaves [2,67].In the wild type 70-15, a large amount of glycogen accumulates in the ungerminated conidia but is immediately degraded during conidial germination.During appressorium development, as the appressorium begins melanism, the abundant glycogen in it begins to degrade [67].Changes in glycogen position during appressorium formation were observed by iodine staining.Large amounts of glycogen were observed in the conidia, germ tubes, and incipient appressoria of wild type 70-15 and the ΔMoswe1 mutant from 0 to 4 h during conidial germination (Fig. S5A and  B).However, the redeployment of glycogen was remarkably retarded in the ΔMoswe1 mutant at 16 hpi.While 80.13% of the glycogen in conidia of wild type 70-15 was transferred into the appressoria, 66.7% of the glycogen in the ΔMoswe1 mutant was not transferred to appressoria (Fig. S5C and D).At 24 hpi, only 41.73% of the glycogen in ΔMoswe1 appressoria had been degraded and utilized, while 95.17% of that in wild type 70-15 appressoria had been degraded and used (Fig. S5C and E).As shown in Fig. S5F-H, consistent glycogen and lipid body utilization and degradation patterns were observed in the ΔMoswe1 mutant.The results indicated that the utilization and degradation of glycogen and lipid bodies are attenuated in the ΔMoswe1 mutant.

Glycogen metabolism, fatty acid metabolism, and autophagy pathways were disturbed in the ΔMoswe1 mutant
Considering that MoSwe1 functions in glycogen metabolism and lipid metabolism progression and influences autophagy, the metabolomic and transcriptomic profiles of ΔMoswe1 and 70-15 were analyzed and compared.Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis indicated that galactose metabolism, fructose, and mannose metabolism, biosynthesis of unsaturated fatty acids, and fatty acid biosynthesis were the most highly enriched pathways (Fig. S6A).A cluster map of the differential metabolites, including fatty acids (alpha-linolenic acid, linoleic acid, tetracosanoic acid, stearic acid, palmitic acid, myristic acid, pentadecanoic acid, 11(Z),14(Z),17(Z)-eicosatrienoic acid) and glycogen (sucrose, maltotriose, D-quinovose, alpha-D-glucose, D-mannose), showed higher levels in the ΔMoswe1 mutant (Fig. S6B).Transcriptome data analysis again indicated that MoSwe1 regulates many metabolic pathways by regulating the expression of the other genes involved in glycerolipid metabolism, mannose type O-glycan biosynthesis, galactose metabolism, glycerophospholipid metabolism, amino sugar and nucleotide sugar metabolism, pentose and glucoronate interconversions, fructose and mannose metabolism, starch and sucrose metabolism, and autophagy (Fig. S6C).

Discussion
The cell cycle is critical for differentiation in eukaryotic cells and must effectively coordinate with cell division to form specific tissues [10,29,66].The Cell wall integrity (CWI) signaling pathway is necessary for maintaining cell morphology and acting as a barrier against extracellular stress [42].At the same time, The autophagy pathway degrades waste organs and other materials so that cells can survive better [80].The association between the autophagy pathway and the CWI pathway was established by phosphorylation of the CWI pathway protein MoMkk1 by the autophagy protein MoAtg1 in M. oryzae [79].The CWI pathway protein MoMkk1 was phosphorylated by Mitotic Exit Network (MEN) protein MoSep1 to link the cell cycle pathway to the CWI pathway in M. oryzae [13].However, the relationship between autophagy, CWI, and cell cycle pathways remains unclear.In our study, we found that a cell cycle kinase, MoSwe1, phosphorylates the CWI pathway MoMps1, linking the CWI pathway to the cell cycle pathway.In addition, MoSwe1 interacts with MoAtg17 and MoAtg18 to affect autophagy pathways, linking cell cycle pathways to autophagy pathways.phosphoproteomic data also showed significant changes in the phosphorylation levels of autophagy pathway associated proteins, CWI associated proteins, and mitosis associated proteins in the ΔMoswe1 mutant.MoSwe1 connects cell cycle pathway, CWI pathway, and autophagy pathway in series.More importantly, the absence of MoSWE1 seriously affected the infection and pathogenicity of M. oryzae.
Swe1-related kinase function through a highly conserved mechanism that controls the timing of entry into mitosis and monitors cell size or growth [27].In S. cerevisiae, ∆swe1 cells undergo premature entry into mitosis before sufficient growth of the daughter bud has occurred, producing abnormally small cells [20].Swe1 regulates the G2/M transition in S. cerevisiae [7].Studies have shown that the Swe1-lacking mutant does not enter mitosis in advance in budding yeast [7,63].Studies in fission yeast and Xenopus have shown that mutants enter mitosis prematurely [51,71].Compared with the results obtained thus far for model organisms in yeast and animals, our finding here revealed that the M. oryzae homologs of SWE1, namely, MoSWE1, play a primary role in phase progression from G1 to S but not the other phases.This novel discovery is confirmed by the following results.HU treatment triggers the S phase checkpoint and arrests cells in S phase [34].In our study, the ΔMoswe1 mutant and wild-type strain 70-15 showed no difference when treated with HU.Similarly, Swe1 mutants in yeast did not show obvious HU sensitivity [34].We speculated that MoSwe1 does not directly act on the S phase to regulate DNA synthesis.In fission yeast, a certain proportion of Δswe1 mutant cells were multinucleated, with some having as many as eight nuclei [20].The number of conidial septa and nuclei in each conidial cell was increased in the ΔMoswe1 mutant.The cells generally exhibited two nuclei; some conidia had up to eight nuclei.Using chromosomal tags, we also examined whether the cells were in the G1 or S/G2 phase of the cell cycle.We found that all cells of the conidia in the ΔMoswe1 mutant entered the S phase, not just the apical cells, and the appressoria also entered the S phase again to replicate, forming four GFP spots.This finding suggested that knocking out MoSWE1 leads to premature entry into the S phase, and excessive mitosis leads to developmental abnormalities.MoSwe1 is similar to the switch of the mitotic process.After MoSWE1 knockout, the mitotic process of the rice blast fungus was uncontrolled, and the fungus continued to divide.Therefore, we concluded that MoSwe1 regulate the G1/S phase transition in cell cycle progression of M. oryzae.
Swe1 plays a crucial role in morphogenesis checkpoints that delay cell cycle progression in response to defects in bud formation [39,47].In M. oryzae, the S phase is essential for the differentiation of the initial appressorium, while the M phase is necessary to develop the functional appressoria that form the penetration peg [61].We found that the conidial morphology of the ΔMoswe1 mutant was abnormal; most of the conidia were longer, and the number of conidial septa was increased, with three-cell conidia in wild type 70-15 and up to 4/5/6 cells in one conidium of the ΔMoswe1 mutant.In addition, the appressoria of the ΔMoswe1 mutant were smaller in size than the appressoria of 70-15.MoSwe1 might play an essential role in monitoring cytoskeletal organization in M. oryzae.
Swe1 is essential for mitosis, but other specific functions of Swe1 in pathogenic plant fungi are still unclear.The absence of any CWI MAPK cascade component has resulted in reduced pathogenicity of M. oryzae.The CWI pathway is necessary for the hyphae morphogenesis and infection process of M. oryzae [78].Cell cycle-related proteins are also essential for maintaining appressorium development and pathogenicity in M. oryzae [17,62].Pkc1 (CWI pathway-associated protein) negatively regulates the cell cycle G2/M transcriptional program [18].CWI pathway is activated during the budding process and inactivated in the G2/M transition [30,43].Here, we discovered that the ΔMoswe1 mutant was more resistant to cell wall stress.MoSwe1 interacted with MoMps1.MoSwe1 affected MoMps1 phosphorylation by phosphorylating MoMps1 at the thr185 site and tyr187 site.
Autophagy is a highly conserved catabolic pathway that uses the autophagosome to enclose cellular materials and fuse them with lysosomes to degrade them, then release and recycle them to support cell metabolism [33].Studies have shown that autophagy activity is reduced during mitosis in human cells.Cyclin-dependent kinase inhibitors (CDKI) and retinoblastoma protein (Rb)/E2 factor (E2F) regulate autophagy activity [4,43].Here, we found that MoSwe1 interacts with MoAtg17 and MoAtg18.The phosphorylation levels of MoAtg1 and MoAtg18 were significantly down-regulated in the ΔMoswe1 mutant.In the ΔMoswe1 mutant, the autophagy process was markedly accelerated since the content of MoAtg8-PE was increased considerably.Our results suggested that MoSwe1 negatively regulates autophagy by promoting the phosphorylation levels of MoAtg17 and MoAtg18.
In M. oryzae, the assembly of septin and the establishment of the F-actin network are necessary for the rice blast fungus to rupture the leaf cuticle plant [11].In the ΔMoswe1 mutant, the frequency of the septin ring was lower than that in the wild type 70 − 15.The results indicated that the attenuated assembly of septin in the ΔMoswe1 mutant decreased the cortical rigidity at the appressorium pore enough that the fungus could not penetrate the host cuticle.In M. oryzae, from conidium to appressorium formation, mitosis is always accompanied by programmed cell death of the conidia [68].Lipid and glycogen stores in the conidia are mobilized and transported to the appressorium during appressorium development in M. oryzae.Previous studies have indicated lipid metabolism and the glyoxylate cycle are necessary for appressorium formation rather than sugar metabolism [5,6,55,57,72,73].Richard A. Wilson proved that TKL1, encoding transketolase, is required for a metabolic checkpoint to control the cell cycle and hyphal growth in M. oryzae [14].ABL1 acts as a glucose signal component to regulate cell cycle tuning and mediate the terminal appressorium of the cell differentiation in M. oryzae [44].In the ΔMoswe1 mutant, the mobilization of glycogen and lipids was notably retarded.At 24 hpi, undegraded glycogen and lipids remained in the conidia in the ΔMoswe1 mutant.Metabolomics and transcriptome data showed that glycogen and fatty acid metabolism in the ΔMoswe1 mutant significantly differed from those in the wild type 70-15.These data indicated that MoSWE1 is related to glycogen and fatty acid metabolism.However, how MoSwe1 specifically responds to sugar metabolism, fatty acid, or energy metabolism to regulate the cell cycle remains to be further studied.
The Nicholas J. Talbot laboratory has certified that rice blast fungus infection is controlled by two unrelated S-phase checkpoints that operate in two consecutive cell cycles in the blast fungus [53].Only when the second round of mitosis proceeds normally can the penetration peg elongate and breach the cuticle of the leaves [52].In our study, the appressorial collapse rate of the ΔMoswe1 mutant was strikingly higher than that of wild type 70-15, indicating that the turgor pressure in the appressorium was affected in the ΔMoswe1 mutant, which further affected plant infection.Therefore, nearly no invasive hyphae were formed after 48 h of induction on the leaves treated with the ΔMoswe1 mutant, and thus, the ΔMoswe1 mutant is nearly nonpathogenic.In previous research, Osés-Ruiz et al. speculated that in the process of plant penetration mediated by appressoria in M. oryzae, there might be a close relationship between turgor generation, cytoskeletal reorganization, and cell cycle progression by the MoSwe1 kinase [52].These data indicated that MoSwe1 regulates the turgor pressure, which is dependent on the second round of the cell cycle.
In conclusion, the study of MoSwe1 regulating MoMps1 phosphorylation reveals a new mechanism by which the cell cycle and CWI pathway coordinate to influence the pathogenesis of M. oryzae.Meanwhile, the interaction of MoSwe1 with MoAtg17 and MoAtg18 revealed the coordination of the cell cycle and autophagy to regulate the pathogenesis of M. oryzae (Fig. 10).Such a conclusion implies that the function of the cell cycle in response to the CWI pathway and autophagy plays an integral part in the growth and pathogenicity of the rice blast fungus.Given such an important role, further study of cell cycle-CWI-autophagy crosstalk is imperative.

Strains and cultural conditions
The wild-type strain of M. oryzae applied for this study was 70-15.Strains were grown on CM in a constant temperature (25°C) incubator alternating between 16 h of light and 8 h of darkness [54] unless indicated otherwise.

MoSWE1 gene disruption and complementation
We constructed MoSWE1 knockout vectors according to a previously described protocol [8,40].Primers (Table S1) were used to amplify upstream (~ 1000 bp) and downstream (~ 1000 bp) segments from the wild type 70 − 15.Special primers were applied to magnify the BAR (glufosinate acyltransferase) sequence from pCB1003 [36].The pKO1B vector was cut open with a restriction endonuclease, and then the three recovered purified fragments (upstream, downstream, BAR) were joined to the cut vector by fusion enzyme (Vazyme, China) [8].The correctly constructed knockout vector verified by PCR was used to transform 70 − 15 via Agrobacterium tumefaciens-mediated transformation (ATMT).The number of copies of the BAR gene in the mutant was detected by the fluorescent quantitative PCR (qPCR) method to determine whether the knockout mutant was a singlecopy mutant.A single copy of the tubulin gene was used as a positive control.The data were computed according to a previous method [40].To produce a ΔMoswe1-C, a MoSWE1 gene containing an approximately 2000 bp promoter sequence was amplified and cloned into pKD5 [8].

Mutant phenotyping experiments
For M. oryzae vegetative growth, small blocks of strains were cultured on CM medium plates for 8 days and then measured and analyzed.We used a previously described CFW staining method to assess conidial morphology to observe conidia separation [19].The wild type 70-15 and the ΔMoswe1 mutant were cultured on solid CM medium for 6 days at 25°C.The edge of the colony was selected to obtain a fungus cake by using a hole punch, and the cake was placed on a 9 cm petri dish and cultured for 11 days.Conidia were washed with distilled water and collected by centrifugation.The number of conidia was counted under the microscope with a hemocytometer.To assess conidial germination and appressorium formation of M. oryzae, 20 µl of conidial suspension (5 × 10 4 conidia/ml) was inoculated onto a hydrophobic plastic surface and incubated in a humid box at 25°C in the dark.The assays were repeated independently three times, with three replicates each time.For the virulence test of M. oryzae, 20 µl of conidial suspensions (1 × 10 5 conidia/ ml) was dripped on susceptible rice seedling leaves and one-week-old barley leaves.In addition, isolated barley leaves were inoculated with mycelial plugs for 4 days.1 × 10 5 conidia/ml conidial suspensions were dropped on detached barley leaves at 25°C for the plant infection assays.The infection of barley leaves after 48 h of induction was surveyed with a Nikon microscope.

Fluorescence observation
To study nuclear division, the nuclear localization signal with red fluorescence (NLS-mCherry) was diverted to M. oryzae wild type 70-15, the ΔMoswe1 mutant, and the ΔMoswe1-C.The nuclear distribution in conidia and during appressorium development was observed by laser confocal microscopy (LSM880).

Cytorrhysis analysis and HU assays
Mature appressoria were placed in glycerol at different concentrations, and at least 100 appressoria were tested in M. oryzae at each concentration.For HU treatment, 200 mM HU was added 2 h after the induction of appressoria, and appressorium formation was observed 24 h after induction in M. oryzae [18].

Strains expressing GFP fusion protein for chromosome tagging
The chromosomal tag was obtained by simultaneously transforming the plasmid encoding the GFP-Lac repressor protein with the nuclear localization signal (pBITEF-GFPLacIN) into the M. oryzae wild type 70-15, the ΔMoswe1 mutant together with the plasmid encoding a collection of 256 lac operator repeats (pCTLacOS) [16].Protoplasts were transformed as described previously [36].

Quantitative real-time PCR (qPCR) methods
Wild type 70-15 and ΔMoswe1 mutant strains were shaken and cultured in CM liquid medium for 48 h, the mycelia were collected, and the RNA was extracted after grinding with liquid nitrogen and reverse transcribed into cDNA.cDNA samples can be directly used in qPCR.We used a real-time PCR instrument (Eppendorf, Germany) to perform quantitative real-time PCR (qPCR) with ChamQ SYBR qPCR Master Mix (Vazyme, China) and measured gene expression levels according to the manufacturer's guidelines.We utilized 2 −∆∆CT to calculate the gene expression level difference between the wild type and mutant, and 40S and α-ACTIN genes were used as controls [38].Duncan's test evaluated significant differences between samples for all experimental data.

In vitro pull-down assays
MoSwe1-N2 was amplified from the cDNA of MoSwe1 and ligated to the vector PGEX4T-1 to obtain the MoSwe1-N2-GST plasmid.MoAtg17 and MoAtg18 were amplified from the cDNA of M. oryzae and ligated to the vector pET-32a to obtain the MoAtg17-His and MoAtg18-His plasmids.The MoSwe1-N2-GST, MoAtg17-His, and MoAtg18-His plasmids were transformed into the expression E. coli strain (DE3 + Plyse), IPTG (4mM) was added, and the expression of the three proteins was detected after overnight culture at 18°C.GST magnetic beads were used to pull MoSwe1-N2-GST protein, which was enriched on the magnetic beads, and MoAtg17-His or MoAtg18-His were added and eluted.MoAtg17-His or MoAtg18-His was detected by an anti-His antibody in an elution buffer (HuaBio, China).

Western blot assays
The fungal hyphae were shaken using liquid CM for two days and then transferred to SD-N medium (0.17% yeast nitrogen base without amino acids and ammonium sulfate, 2% glucose) for an additional 4 h of nitrogen starvation induction to triggering autophagy.Western blot detection of GFP-MoAtg8 fusion protein with GFP antibody (GFP 1:10,000-20000; Abcam).To detect endogenous MoAtg8/MoAtg8-PE, 70-15 and the ΔMoswe1 mutant were cultivated in liquid CM for 48 h and then rapidly transferred to SD-N medium for 3 or 6 h.The protein was extracted by the TCA method, and an anti-Atg8 antibody (Atg8 1:500-1,000; MBL) was used to detect MoAtg8 and MoAtg8-PE levels.
Total proteins were isolated by TCA-acetone methods to assay the phosphorylated Mps1 levels.We used an anti-P-p44/42 antibody (Cell Signalling Technology) and an anti-p44/42 MAPK antibody (Cell Signalling Technology) as controls.Total proteins were extracted from hyphae grown in liquid CM to detect phosphorylated Cdc2.We used an anti-cdc2 antibody (Santa Cruz Biotechnology) and Phospho-cdc2 (Tyr15) antibody (Cell Signalling Technology) to detect nonphosphorylated and phosphorylated Cdc28 levels, respectively.

Fig. 1
Fig. 1 MoSwe1 interacts with MoCdc28 to affect its phosphorylation level.A BiFC was used to detect the interaction relationship between MoSwe1 and MoCdc28.The YFP signals can be observed in MoSwe1-YFPN and MoCdc28-YFPC co-transformed strains: scale bar, 5 μm.B Yeast two-hybrid analysis to examine the interaction of MoSwe1-N2 and MoCdc28 in vivo.The positive control was pGBKT7-53 and PGADT7-T.Pairs of pGBKT7 and AD-MoSwe1-N2 and pGADT7 and BD-MoCdc28 were negative controls.C Detection of the Cdc28 phosphorylation in the ΔMoswe1 mutant.Western blot was carried out to detect Cdc28 Y15 (for phosphorylation signal) and Cdc28 in protein extracts using the anti-phospho-Cdc28 (Tyr15) and anti-Cdc28 antibodies, respectively

Fig. 2 Fig. 3
Fig. 2 MoSwe1 functions in the cell cycle and regulates G1/S progression in M. oryzae.A Visualization of nuclei during appressorium development using NLS-mCherry.The merged image shows NLS-mCherry and DIC: bars, 10 μm.B The number of occurrences of two nuclei in one cell of the conidium during conidial germination.C The number of nuclei in conidia during conidial germination.D The number of nuclei in appressoria during conidial germination.E Degradation of H2B-mCherry was examined in 70-15 and ΔMoswe1.The 70-15 and ΔMoswe1 strains with H2B-mCherry tags were induced in SD-N medium for 0, 3, and 6 h, respectively.The degradation level of mCherry was detected by western blotting using mCherry antibodies

Fig. 4
Fig. 4 MoSwe1 is indispensable for fungal vegetative growth, appressorium formation, conidiogenesis, conidial production, and appressorial morphology in M. oryzae.A 70-15, ΔMoswe1 and ΔMoswe1-C strains were grown on CM, MM, OMA, and V8 medium for 8 days.B Diameters of colonies.Duncan's test (**, P < 0.01).C Appressorium formation was induced by a hydrophobic surface: scale bar, 10 μm.D Compute appressorium formation rate and perform statistical analysis.Asterisks delegate significant differences (P < 0.01).E Statistical analysis of conidial production.F Stained conidial septa of 70-15, ΔMoswe1 and ΔMoswe1-C with CFW.Bars, 10 μm.G Number of conidial cells in 70-15, ΔMoswe1 and ΔMoswe1-C.H Images of the appressorium were taken using a light microscope.Samples were incubated to induce appressoria in the 70-15, ΔMoswe1 mutant and ΔMoswe1-C strains: scale bar, 10 μm.I Measurement of the diameter of the appressorium.The experiment was repeated three times with three replicates per treatment.Significant differences were calculated using Duncan's test.Asterisks denote statistical significance (P < 0.01)

Fig. 5
Fig. 5 MoSwe1 contributes to virulence in M. oryzae.A Conidial suspensions (1 × 10 5 conidia/ml) of the 70-15, ΔMoswe1 and ΔMoswe1-C strains were dropped on two-week-old rice seedlings.B Conidial suspensions (1 × 10 5 conidia/ml) of the 70-15, ΔMoswe1, and ΔMoswe1-C were dropped onto barley leaves in vitro.C Disease incidence on isolated barley leaves inoculated with mycelial plugs of the 70-15, the ΔMoswe1 and ΔMoswe1-C strains.D Rice seedlings (2 weeks old) inoculated with conidial (5 × 10 4 conidia/ml) suspensions of 70-15, ΔMoswe1 and ΔMoswe1-C.Evaluation of disease spots on rice leaves was carried out at 7 dpi.E The lesion areas were counted and calculated using Adobe Photoshop CC.F and G Artificial division of the types of IH into four types.At least 100 IH of each strain were tallied.Scale bar, 10 μm.H and I Cell collapse experiments were performed with 0.5-2 M glycerol concentrations, and at least 100 appressoria were tallied for each concentration.Asterisks denote statistical significance (P < 0.01)

Fig. 6
Fig. 6 MoSwe1 interacts with MoAtg17 and MoAtg18.A and D Pull-down assays.GST magnetic beads were used to pull down MoSwe1-N2-GST protein, which was enriched on the magnetic beads, and MoAtg17-His or MoAtg18-His was added and eluted.Anti-His and anti-GST antibodies in elution buffer detected the presence of MoAtg17-His or MoAtg18-His.B and E Yeast two-hybrid experiment to test the interaction between MoSwe1 and MoAtg17 and MoAtg18.C and F BiFC experiment to test the interaction between MoSwe1 and MoAtg17 and MoAtg18.Scale bar, 5 μm

Fig. 9
Fig. 9 MoSwe1 affects the CWI pathway by regulating MoMps1 phosphorylation.A 70-15, the ΔMoswe1 mutant, and ΔMoswe1-C on CM with 0.005% SDS, 400 µg/ml Congo Red (CR) were cultured for 8 days, and pictures were taken.B The relative inhibition rates of 70-15, ΔMoswe1 mutant, and ΔMoswe1-C were calculated in triplicate.Asterisks are used to indicate statistically significant differences (**P < 0.01).C The phosphorylation level of Mps1 in 70-15 and the ΔMoswe1 mutant was assayed.D Phosphoproteomic data showed that MoMps1 phosphorylation levels at 186T and 188Y were significantly down-regulated.E and F AlphaFold predict Mps1 of M. oryzae and human homologous Mps1 and intercept amplification near the phosphorylation site.G BiFC experiment verifies the interaction between MoMps1 and MoSwe1.Scale bar, 5 μm.H The interaction between MoMps1 and MoSwe1 was verified by a yeast two-hybrid experiment

Fig. 10 A
Fig. 10 A proposed model for the MoSwe1 function.In the process of M. oryzae infection, it faces various stresses from the external environment and rice.MoSwe1, as a mitotic protein kinase, is involved in regulating the G1 to S phase of M. oryzae mitosis but not other phases.Swe1 negatively regulates autophagy by interacting with MoAtg17 and MoAtg18.MoSwe1 affects MoMps1 phosphorylation and thus regulates the conidiation and CWI pathway of M. oryzae.MoSwe1 connects the cell cycle, CWI pathway, and autophagy to coordinate the regulation of the pathogenicity of M. oryzae